- SUNY Upstate Medical University (Syracuse, NY)
- …with study participants. Adhere to IRB approved protocols, comply with Institutional policies, SOP guidelines, and federal , state, and sponsor policies. ... Job Summary: The Department of Emergency Medicine conducts a wide range of research studies at University Hospital. We are looking for a personable, self-motivated… more
- University of Pennsylvania (Philadelphia, PA)
- …the Investigator, sponsor or CRO, includes source documentation, case report forms, and research charts. Collect, review , and report study data. Complete case ... ability to work as part of a team, as well as independently; knowledge of IRB and human research protection regulations. CRC-A + Bachelor of Science and 1… more
- Beth Israel Lahey Health (Boston, MA)
- **Overview** The purpose of the **Clinical Research Coordinator I** is to coordinate clinical research activities for the Joslin 50-year Medalist Study, which ... the Medalist Program. + Identify eligible participants + Inform patients of research and eligibility + Recruiting and scheduling study participants + Assess… more
- City of New York (New York, NY)
- …technical documentation and programs (codebooks, programming syntax, etc.) - Manage IRB review /approval PREFERRED SKILLS: - Advanced degree in epidemiology, ... and wellness promotion, BCDP employs evidence-based policies, programs, communications, and research to advance its objectives, as well as spearheads and evaluates… more
- Mount Sinai Health System (New York, NY)
- **Job Description** The Clinical Research Assistant II performs a wide variety of activities related to clinical research study on behalf of the Tisch Cancer ... Institute, Cancer Clinical Trials, Multiple Myeloma team. The Clinical Research Assistant II supports the Clinical Research Team and PI in their efforts to… more
- Mount Sinai Health System (New York, NY)
- …Under general supervision, analyzes and interprets highly complex clinical research data; conducts clinical testing and develops protocols. Develops work ... trains and reviews the work of less experienced clinical research staff. Oversees the clinical assessments of the study...and negotiation. + May prepare and ensure grant applications, IRB / GCO documents are submitted. + Coordinates protocols… more
- University of Miami (Miami, FL)
- …staff position using the Career worklet, please review this tip sheet (https://my.it.miami.edu/wda/erpsec/tipsheets/ER\_eRecruiting\_ApplyforaJob.pdf) . The Hussman ... Institute has an exciting opportunity for a full time Clinical Research Participant Specialist position. The incumbent assists in community outreach, recruitment,… more
- Kelly Services (New Haven, CT)
- **Project Manager - Imaging Research Services** **Kelly(R) Science & Clinical** is seeking a Project Manager for a direct-hire, hybrid full-time role with an ... innovative research organization in New Haven, CT. If you're passionate...documentation, and action item tracking. + Coordinate regulatory submissions ( IRB ) and ensure project compliance. + Prepare metrics and… more
- Mount Sinai Health System (New York, NY)
- …goals. **Regulatory & Quality Management** + Ensure compliance with FDA, ICH/GCP, IRB , and institutional standards for all study-related activities. + Oversee ... management of clinical trials within the Center for Interventional Cardiovascular Research & Clinical Trials. This role ensures high-quality, efficient study… more
- University of Rochester (Rochester, NY)
- …equity considerations._ **Responsibilities:** Regularly provides routine technical support for research activities and/or laboratory support. Applies full range of ... sampling, maintenance, operation and calibration of scientific monitoring equipment for research projects. Responsible for general data collection and assisting with… more